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• W2913885049 endingPage "339" @default.
• W2913885049 startingPage "333" @default.
• W2913885049 abstract "Abstract Hereditary hemorrhagic telangiectasia (HHT) is a vascular disease characterized by nose and gastrointestinal bleeding, telangiectases in skin and mucosa, and arteriovenous malformations in major internal organs. Most patients carry a mutation in the coding region of the endoglin ( ENG ) or activin A receptor type II-1 ( ACVRL1 ) gene. Nonetheless, in around 15% of patients, sequencing analysis and duplication/deletion tests fail to pinpoint mutations in the coding regions of these genes. In these cases, it has been shown that sequencing of the 5’-untranslated region (5’UTR) of ENG may be useful to identify novel mutations in the ENG non-coding region. Here we report the genetic characterization and functional analysis of the heterozygous mutation c.-142A>T in the 5’UTR region of ENG found in a family with several members affected by HHT. This variant gives rise to a new initiation codon of the protein that involves the change in its open reading frame. Transfection studies in monkey cells using endoglin expression vectors demonstrated that c-142A>T mutation results in a clear reduction in the levels of the endoglin protein. These results support the inclusion of the 5’UTR of ENG in the standard genetic testing for HHT to increase its sensitivity." @default.
• W2913885049 created "2019-02-21" @default.
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• W2913885049 date "2019-02-06" @default.
• W2913885049 modified "2023-10-18" @default.
• W2913885049 title "Characterization of a family mutation in the 5’ untranslated region of the endoglin gene causative of hereditary hemorrhagic telangiectasia" @default.
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• W2913885049 doi "https://doi.org/10.1038/s10038-019-0564-x" @default.
• W2913885049 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8075931" @default.
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